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255399007: Congenital (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
273731000077117 congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
380598010 Congenital en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
380599019 Congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
554801000077113 congénital (valeur de l'attribut) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
congénital est un(e) (attribut) périodes de vie true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
syndrome de pseudo-infection intra-utérine congénitale survenue (attribut) True congénital Inferred relationship Some 2
syndrome de pseudo-infection intra-utérine congénitale survenue (attribut) False congénital Inferred relationship Some 3
Congenital lethal erythroderma (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Ornithinemia with gyrate atrophy survenue (attribut) False congénital Inferred relationship Some
Congenital absence of gastric muscle (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital anomaly of mother complicating pregnancy (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Congenital chalasia of esophagus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital short esophagus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Duplication cyst of esophagus (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Duplication cyst of esophagus (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Congenital infection caused by Echovirus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Mucocutaneous early congenital syphilis (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Arteriovenous malformation of large intestine (disorder) survenue (attribut) False congénital Inferred relationship Some 2
Arteriovenous malformation of large intestine (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Oculocutaneous albinism type 5 (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Oculocutaneous albinism type 6 (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Oculocutaneous albinism type 7 (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Odontoleukodystrophy (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Okamoto syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Congenital nephrotic syndrome due to congenital infection (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Congenital myogenic ptosis survenue (attribut) False congénital Inferred relationship Some
Ocular albinism with late-onset sensorineural deafness (disorder) survenue (attribut) False congénital Inferred relationship Some 8
Oculogastrointestinal muscular dystrophy (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Severe combined immunodeficiency with hypereosinophilia (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Gomez Lopez Hernandez syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Gomez Lopez Hernandez syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Gomez Lopez Hernandez syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 7
Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 8
Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 9
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
syndrome d'agénésie du corps calleux-microcéphalie-petite taille survenue (attribut) True congénital Inferred relationship Some 3
syndrome d'agénésie du corps calleux-microcéphalie-petite taille survenue (attribut) False congénital Inferred relationship Some 4
syndrome d'agénésie du corps calleux-microcéphalie-petite taille survenue (attribut) False congénital Inferred relationship Some 5
Intellectual disability, developmental delay, contracture syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Intellectual disability, developmental delay, contracture syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Intellectual disability, developmental delay, contracture syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Juvenile cataract, microcornea, renal glucosuria syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Matthew Wood syndrome survenue (attribut) True congénital Inferred relationship Some 2
Matthew Wood syndrome survenue (attribut) False congénital Inferred relationship Some 3
Skeletal dysplasia with intellectual disability syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 2
DK phocomelia syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 7
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Juvenile cataract, microcornea, renal glucosuria syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Ganglioside GM3 synthase deficiency (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Congenital keratoconus survenue (attribut) True congénital Inferred relationship Some 1
Congenital keratoconus posticus circumscriptus survenue (attribut) True congénital Inferred relationship Some 1
Sacral dysgenesis survenue (attribut) True congénital Inferred relationship Some 1
Deletion 5q35 survenue (attribut) True congénital Inferred relationship Some 2
Deletion 5q35 survenue (attribut) True congénital Inferred relationship Some 3
Early-onset X-linked optic atrophy (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Ectodermal dysplasia with blindness syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Ectodermal dysplasia with blindness syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 5
Ectodermal dysplasia with blindness syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Ectodermal dysplasia with blindness syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 7
syndrome de Furhmann survenue (attribut) True congénital Inferred relationship Some 2
syndrome de Furhmann survenue (attribut) False congénital Inferred relationship Some 3
Galloway Mowat syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Galloway Mowat syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 7
Oro-facial digital syndrome type 10 (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Oro-facial digital syndrome type 10 (disorder) survenue (attribut) True congénital Inferred relationship Some 5
Oro-facial digital syndrome type 10 (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Oro-facial digital syndrome type 10 (disorder) survenue (attribut) False congénital Inferred relationship Some 7
syndrome oro-facio-digital type 5 survenue (attribut) True congénital Inferred relationship Some 4
syndrome oro-facio-digital type 5 survenue (attribut) True congénital Inferred relationship Some 5
syndrome oro-facio-digital type 5 survenue (attribut) False congénital Inferred relationship Some 6
syndrome oro-facio-digital type 5 survenue (attribut) False congénital Inferred relationship Some 7
Oro-facial digital syndrome type 8 (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) survenue (attribut) True congénital Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) survenue (attribut) False congénital Inferred relationship Some 7
Ossification anomaly with psychomotor developmental delay syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Ossification anomaly with psychomotor developmental delay syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 7
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 8
Osteocraniostenosis (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 4
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 5
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 6
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome survenue (attribut) False congénital Inferred relationship Some 4
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome survenue (attribut) True congénital Inferred relationship Some 5
Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Pacman dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 3

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